510(k) · Cleared
ClearedOsteoSelect PLUS Demineralized Bone Matrix Putty
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Bacterin International, Inc. · MQV Filler, Bone Void, Calcium Compound
Cleared on Aug 18, 2015 as substantially equivalent to K091321 (Bacterin International, Inc., 2009) and 1 other predicate after a 160-day review. Its family tree reaches back 3 generations to 2005.
- Decided
- Aug 18, 2015
- Review
- 160 days
- Class
- Class II
- Product code
- MQV
- Recalls
- None
- Predicates
- 2
Its longest line of descent runs back 3 generations to K040262 (2005). 6 ancestors in all. No later device cites it as a predicate yet.
- Root · 3 generations backK040262 DBX Demineralized Bone Matrix Putty, Bone Matrix Paste and Bone…Musculoskeletal Transplant Foundation · 2005 · Recalled
- 2 generations backK091321 Osteoselect Demineralized Bone Matrix PuttyBacterin International, Inc. · 2009 · Recalled
- 1 generation backK130498 Osteoselect Demineralized Bone Matrix PuttyBacterin International, Inc. · 2013 · Recalled
- This deviceK150621 OsteoSelect PLUS Demineralized Bone Matrix PuttyBacterin International, Inc. · 2015
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K040262 | DBX Demineralized Bone Matrix Putty, Bone Matrix Paste and Bone Matrix Mix | Musculoskeletal Transplant Foundation | 2005 | 2 |
| −2 | K091321 | Osteoselect Demineralized Bone Matrix Putty | Bacterin International, Inc. | 2009 | 2 |
| −1 | K130498 | Osteoselect Demineralized Bone Matrix Putty | Bacterin International, Inc. | 2013 | 1 |
| 0 (this device) | K150621 | OsteoSelect PLUS Demineralized Bone Matrix Putty | Bacterin International, Inc. | 2015 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2005 | 1 | 0 |
| 2011 | 2 | 0 |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
Planning a device in MQV? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new MQV device
- #1 K232315 Catalyst Bone Void Fillerscore 25.2 · 25 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (2)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K091321 | Osteoselect Demineralized Bone Matrix PuttySummary page 5…icate Devices Primary Predicate OsteoSelect® Demineralized Bone Matrix Putty Bacterin International, Inc. K091321 (use in extremities and pelvis) K130498 (use in posterolateral spine) References DBX®… | 2009 |
| * | K130498 | Osteoselect Demineralized Bone Matrix PuttySummary page 5…d Bone Matrix Putty Bacterin International, Inc. K091321 (use in extremities and pelvis) K130498 (use in posterolateral spine) References DBX® MIX Demineralized Bone Matrix Putty Muscu… | 2013 |
| † | K063676 | DBX Demineralized Bone Matrix Mix | 2007 |
| † | K082002 | Progenix Plus | 2008 |
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- The line of descent spans 10 years and passes through 2 companies; a new generation was cleared every 3.7 years on median.
- 4 of the 6 ancestors have a recall of any class.
- 1 other device also cites its predicate K091321.
How does its category compare?
All MQV devicesMQV Filler, Bone Void, Calcium Compound: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.
FDA decisions per year · MQV
14in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · MQV
57in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · MQV
1in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · MQV
57in 2025
MAUDE reports naming product code MQV, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 35 | 144 | 5 | 67 |
| 2008 | 32 | 102 | 3 | 71 |
| 2009 | 23 | 180 | 1 | 81 |
| 2010 | 17 | 147 | 0 | 68 |
| 2011 | 16 | 92 | 6 | 114 |
| 2012 | 9 | 107 | 3 | 149 |
| 2013 | 12 | 197 | 2 | 223 |
| 2014 | 20 | 153 | 0 | 111 |
| 2015 | 18 | 184 | 0 | 125 |
| 2016 | 8 | 214 | 1 | 106 |
| 2017 | 17 | 124 | 1 | 107 |
| 2018 | 23 | 124 | 2 | 86 |
| 2019 | 13 | 90 | 0 | 65 |
| 2020 | 15 | 132 | 1 | 126 |
| 2021 | 8 | 88 | 0 | 101 |
| 2022 | 9 | 118 | 0 | 47 |
| 2023 | 21 | 74 | 3 | 120 |
| 2024 | 28 | 55 | 2 | 68 |
| 2025 | 14 | 57 | 1 | 57 |
| 2026 | 5 | 96 | 4 | — |
What is it indicated for?
OsteoSelect® (DBM) Putty is indicated for use as a bone void filler and bone graft substitute for voids or gaps that are not intrinsic to the stability of the bony structure. OsteoSelect® (DBM) Putty is indicated for treatment of surgically created osseous defects or osseous defects from traumatic injury to the bone.
OsteoSelect® (DBM) Putty can be used as follows:
* Extremities
* Posterolateral spine
* Pelvis
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K150621 · printed Nov 6, 2026
Cite this page
510(k) Report. “K150621: OsteoSelect PLUS Demineralized Bone Matrix Putty.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K150621
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026